Evidence map›Paper›PMID 31744914›Full record

ArticlemBio2019

Gene Regulation Shifts Shed Light on Fungal Adaption in Plant Biomass Decomposers.

Jiwei Zhang, Kevin A T Silverstein, Jesus David Castaño, Melania Figueroa, Jonathan S Schilling

Open access · goldAbstract read
In one paragraph

Article in mBio, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
10.8field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

29 citing papers in PubMed, 58 citations in OpenAlex.

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  13. Comparative Analysis ofInternational journal of molecular sciences · 2022
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  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 1 institution in 2 countries.

Jiwei ZhangDepartment of Plant and Microbial Biology, University of Minnesota, Saint Paul, Minnesota, USA.
Kevin A T SilversteinMinnesota Supercomputing Institute, University of Minnesota, Minneapolis, Minnesota, USA.
Jesus David CastañoDepartment of Plant and Microbial Biology, University of Minnesota, Saint Paul, Minnesota, USA.
Melania FigueroaDepartment of Plant Pathology, University of Minnesota, Saint Paul, Minnesota, USA.
Jonathan S SchillingDepartment of Plant and Microbial Biology, University of Minnesota, Saint Paul, Minnesota, USA schillin@umn.edu.
University of Minnesota · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fungi dominate the recycling of carbon sequestered in woody biomass. This process of organic turnover was first evolved among "white rot" fungi that degrade lignin to access carbohydrates and later evolved multiple times toward more efficient strategies to selectively target carbohydrates-"brown rot." The brown rot adaption was often explained by mechanisms to deploy reactive oxygen species (ROS) to oxidatively attack wood structures. However, its genetic basis remains unclear, especially in the context of gene contractions of conventional carbohydrate-active enzymes (CAZYs) relative to white rot ancestors. Here, we hypothesized that these apparent gains in brown rot efficiency despite gene losses were due, in part, to upregulation of the retained genes. We applied comparative transcriptomics to multiple species of both rot types grown across a wood wafer to create a gradient of progressive decay and to enable tracking temporal gene expression. Dozens of "decay-stage-dependent" ortho-genes were isolated, narrowing a pool of candidate genes with time-dependent regulation unique to brown rot fungi. A broad comparison of the expression timing of CAZY families indicated a temporal regulatory shift of lignocellulose-oxidizing genes toward early stages in brown rot compared to white rot, enabling the segregation of oxidative treatment ahead of hydrolysis. These key brown rot ROS-generating genes with iron ion binding functions were isolated. Moreover, transcription energy was shifted to be invested on the retained GHs in brown rot fungi to strengthen carbohydrate conversion. Collectively, these results support the hypothesis that gene regulation shifts played a pivotal role in brown rot adaptation.

Indexed as

Adaptation, BiologicalBiomassGene Expression Regulation, FungalBiodegradation, EnvironmentalComputational BiologyFungal ProteinsFungiGene Expression ProfilingHydrolysisPlantsWoodFungal Proteinsbrown rot adaptioncomparative transcriptomicsgene regulation shiftplant biomaswood-decomposing fungi

Identifiers

PMID31744914
PMCPMC6867892
OpenAlexW2986099826

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.